EP4394002A1 - Particule électrophorétique et procédé de préparation associé et son application - Google Patents

Particule électrophorétique et procédé de préparation associé et son application Download PDF

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Publication number
EP4394002A1
EP4394002A1 EP22906662.6A EP22906662A EP4394002A1 EP 4394002 A1 EP4394002 A1 EP 4394002A1 EP 22906662 A EP22906662 A EP 22906662A EP 4394002 A1 EP4394002 A1 EP 4394002A1
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EP
European Patent Office
Prior art keywords
core
electrophoretic
particles
particle
shell layer
Prior art date
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EP22906662.6A
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German (de)
English (en)
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EP4394002A4 (fr
Inventor
Zirong WU
Junbin HONG
Hongling Wang
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Shenzhen AV Display Co Ltd
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Shenzhen AV Display Co Ltd
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Application filed by Shenzhen AV Display Co Ltd filed Critical Shenzhen AV Display Co Ltd
Publication of EP4394002A1 publication Critical patent/EP4394002A1/fr
Publication of EP4394002A4 publication Critical patent/EP4394002A4/fr
Pending legal-status Critical Current

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    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/36—Compounds of titanium
    • C09C1/3607—Titanium dioxide
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    • C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
    • C09C3/006—Combinations of treatments provided for in groups C09C3/04 - C09C3/12
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00—Silicon; Compounds thereof
    • C01B33/113—Silicon oxides; Hydrates thereof
    • C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • C01B33/18—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof
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    • C01G23/00—Compounds of titanium
    • C01G23/04—Oxides; Hydroxides
    • C01G23/047—Titanium dioxide
    • C01G23/053—Producing by wet processes, e.g. hydrolysing titanium salts
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    • C01G23/04—Oxides; Hydroxides
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    • C01G23/08—Drying; Calcining ; After treatment of titanium oxide
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    • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0001—Post-treatment of organic pigments or dyes
    • C09B67/0004—Coated particulate pigments or dyes
    • C09B67/0007—Coated particulate pigments or dyes with inorganic coatings
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    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/02—Compounds of alkaline earth metals or magnesium
    • C09C1/028—Compounds containing only magnesium as metal
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    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/28—Compounds of silicon
    • C09C1/30—Silicic acid
    • C09C1/3009—Physical treatment, e.g. grinding; treatment with ultrasonic vibrations
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    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/28—Compounds of silicon
    • C09C1/30—Silicic acid
    • C09C1/3045—Treatment with inorganic compounds
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    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/28—Compounds of silicon
    • C09C1/30—Silicic acid
    • C09C1/309—Combinations of treatments provided for in groups C09C1/3009 - C09C1/3081
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    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
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    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
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    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/36—Compounds of titanium
    • C09C1/3692—Combinations of treatments provided for in groups C09C1/3615 - C09C1/3684
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    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/40—Compounds of aluminium
    • C09C1/407—Aluminium oxides or hydroxides
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    • C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
    • C09C3/04—Physical treatment, e.g. grinding or treatment with ultrasonic vibrations
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    • C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
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    • C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
    • C09C3/06—Treatment with inorganic compounds
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    • C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
    • C09C3/10—Treatment with macromolecular organic compounds
    • G—PHYSICS
    • G02—OPTICS
    • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/165—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on translational movement of particles in a fluid under the influence of an applied field
    • G02F1/166—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on translational movement of particles in a fluid under the influence of an applied field characterised by the electro-optical or magneto-optical effect
    • G02F1/167—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on translational movement of particles in a fluid under the influence of an applied field characterised by the electro-optical or magneto-optical effect by electrophoresis
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    • C01—INORGANIC CHEMISTRY
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    • C01P2004/60—Particles characterised by their size
    • C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
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    • C01P2004/00—Particle morphology
    • C01P2004/80—Particles consisting of a mixture of two or more inorganic phases
    • C01P2004/82—Particles consisting of a mixture of two or more inorganic phases two phases having the same anion, e.g. both oxidic phases
    • C01P2004/84—Particles consisting of a mixture of two or more inorganic phases two phases having the same anion, e.g. both oxidic phases one phase coated with the other
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    • C01P2004/82—Particles consisting of a mixture of two or more inorganic phases two phases having the same anion, e.g. both oxidic phases
    • C01P2004/84—Particles consisting of a mixture of two or more inorganic phases two phases having the same anion, e.g. both oxidic phases one phase coated with the other
    • C01P2004/88—Thick layer coatings
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    • G—PHYSICS
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    • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/165—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on translational movement of particles in a fluid under the influence of an applied field
    • G02F1/1675—Constructional details
    • G02F2001/1678—Constructional details characterised by the composition or particle type

Definitions

  • the application relates to the technical field of electrophoretic particles, and more particularly to an electrophoretic particle, a preparation method therefor, and an application thereof.
  • electrophoretic display technology Due to advantages of energy saving or low energy consumption, good sunlight readability, low production cost, and flexible manufacturing, electrophoretic display technology has stood out from many display technologies and has become one of flexible electronic display technologies having great development potentials.
  • the display principle of the electrophoretic display technology is that charged electrophoretic particles of different colors move under the action of an electric field, thus displaying a desired pattern.
  • Electrophoretic particles in core-shell structures can effectively reduce a density thereof making the density of the electrophoretic particles closer to the density of an electrophoretic fluid, so that the electrophoretic particles have the advantages of excellent bistability and short response time, making them very popular.
  • Core-shell structured particles generally adopt two display modes, that is, core display mode and shell layer display mode.
  • core display mode the existence of a transparent shell layer often results in serious light leakage, thus the core-shell structured particles generally adopt the shell layer display mode.
  • shell layer display mode high requirements are imposed on the properties and thickness of the shell layer material.
  • An object of the present application is to provide an electrophoretic particle and a preparation method therefor and an application thereof, aiming at solving the problems in the prior art that the electrophoretic particle having the core-shell structure cannot well control the thickness of the shell layer, resulting in poor stability and poor use effect of the particle.
  • the present application provides an electrophoretic particle.
  • the electrophoretic particle comprises a shell layer and a core layer wrapped in the shell layer.
  • the core layer comprises a plurality of core particles, and the density of the core particles is lower than that of the shell layer.
  • voids exist among the plurality of core particles.
  • a volume of the core layer accounts for 30% to 80% of a volume of the electrophoretic particle.
  • the density of the plurality of core particles is lower than or equal to a half of the density of the shell layer.
  • the density of the plurality of core particles is 1 g/cm 3 to 2.8g/cm 3 .
  • the electrophoretic particle has a particle size of 300 nm to 1000 nm.
  • each of the plurality of core particles has a particle size of 10 nm to 50 nm.
  • a material of the shell layer has a visible light reflectivity of greater than 70%, or the material of the shell layer has a visible light absorptivity of greater than 80%.
  • the material of the shell layer comprises an inorganic pigment
  • the core particles comprise inorganic particles or organic particles.
  • a material of the inorganic particle comprises silicon dioxide.
  • a material of the organic particles comprises at least one of polymethylmethacrylate, polystyrene, and polyvinylpyrrolidone.
  • the precursor material comprises any one or more of ethyl titanate, isopropyl titanate, tetrabutyl titanate, titanium tetrachloride, zirconium propanol, ferric chloride, ferrous sulfate, zinc nitrate, zinc chloride, zinc sulfate, copper nitrate, and chromium nitrate.
  • the first core particle dispersion is further subjected to an ultrasonic treatment, wherein a duration for the ultrasonic treatment is 20 mins to 2 hrs.
  • a rate of the dropping is controlled at 0.1 mL/s to 0.12 mL/s.
  • a temperature of the mixing and heating reaction is 50°C to 55°C.
  • the present application provides an electrophoretic display liquid.
  • the electrophoretic display liquid comprises electrophoretic particles, in which, the electrophoretic particles are selected from the above-mentioned electrophoretic particles or prepared by the above-mentioned method for preparing the electrophoretic particles.
  • the electrophoretic particle provided by the first aspect of the embodiments of the present application includes the shell layer and the core layer wrapped in the shell layer, the core layer includes the plurality of core particles, and the structure of the plurality of the core particles makes the shell layer wrapping on surfaces of the plurality of the core particles form a folded structure, thus increasing a surface area of the core layer; moreover, the number of groups on the surfaces of the core particles and the corresponding binding groups on the shell layer increases, which improves the bonding tightness between the shell layer and the core layer, and makes the shell layer of the resulting electrophoretic particle have relatively strong tightness.
  • the core particle dispersion having the saturated concentration and the precursor material mixed solution used for preparing the shell layer are separately provided, and the core particle dispersion having the saturated concentration is dropped into the precursor material mixed solution having a relatively low concentration, the particle dispersion does not diffuse rapidly, so that the high concentration solution and the low concentration solution are mixed into a homogeneous solution, and it can be ensured that electrophoretic particles each containing multiple core particles are formed.
  • Both the two preparation ways are simple, convenient, and easy to operate. By using the preparation method, electrophoretic particles being sensitive in movement and having strong dispersion stability without light leakage can be prepared, which is suitable for large-scale preparation.
  • the electrophoretic display liquid provided by the third aspect of the present application includes the above-mentioned electrophoretic particles that are sensitive in movement and have strong dispersion stability without light leakage. Therefore, the obtained electrophoretic display liquid has excellent performance and is conducive to wide application.
  • FIG. 1 is a schematic diagram of a preparation method of electrophoretic particles provided by embodiments of the present application.
  • the term "and/or" describes the association relationship of associated objects, indicating that there may be three relationships, for example, A and/or B may mean the following conditions: A exists alone, A and B exist simultaneously, and B exists alone, in which, A and B can be singular or plural.
  • the character "/" generally indicates that the associated objects are in an "or” relationship.
  • first and second are only used for descriptive purposes to distinguish objects such as substances from each other, and cannot be understood as indicating or implying relative importance or implicitly specifying the quantity of indicated technical features.
  • a first XX can also be called a second XX
  • a second XX can also be called a first XX.
  • a feature defined as “first” and “second” may explicitly or implicitly include one or more of these features.
  • an overall particle size of each electrophoretic particle can be appropriately reduced, the moving velocity of the electrophoretic particle under the action of the electric field can be improved, and it is ensured such electrophoretic particle will never have the light leakage problem.
  • the density of the plurality of core particles is lower than the density of the shell layer, which makes the density of the prepared electrophoretic particle even smaller, thereby slowing down a deposition velocity of the electrophoretic particle when the electric field is removed, improving the dispersion stability of the electrophoretic particles, and making a resulting device have a better steady-state effect.
  • a volume of the voids account for 5% to 15% of a volume of the core layer.
  • the density and stability of the core layer are further controlled. If the volume ratio of the voids in the core layer is smaller, the density of the core layer is greater, and the stability of the resulting core layer is higher; and if the volume ratio of the voids in the core layer is larger, the density of the core layer is smaller, while the stability of the resulting core layer is correspondingly lowered, and the core layer has a potential risk of collapsing, which is not conducive to the formation of electrophoretic particle.
  • the density of the shell layer is 3 g/cm 3 to 5.6 g/cm 3 .
  • the shell layer is mainly used for display, and those skilled in the art can choose appropriate color-developing materials for different display needs, but for the same color display, the lower the density of the material, the lower the density of the prepared electrophoretic particle.
  • the density of the plurality of core particles is 1 g/cm 3 to 2.8g/cm 3 .
  • the density of the plurality of core particles is 1 g/cm 3 to 2.8g/cm 3 .
  • it is conductive to reducing the density of the electrophoretic particle, improving the dispersion stability of the electrophoretic particles, and making the resulting device have a better steady-state effect.
  • the matching degree and the binding stability between the core particles and the shell layer should also be considered.
  • the electrophoretic particle has a particle size of 300 nm to 1000 nm, such that the electrophoretic particles can move rapidly under the action of an electric field, ensuring excellent properties of the prepared device. Under the action of the electric field, if the particle size of the electrophoretic particle is too large, the moving velocity of the electrophoretic particle will be too slow, which will easily lead to poor display effect of the device, which is not conducive to use.
  • the particle size of each of the plurality of core particles is 10 nm, 15 nm, 20 nm, 25 nm, 30 nm, 35 nm, 40 nm, 45 nm, or 50 nm.
  • the core particle dispersion and the precursor material mixed solution for preparing the shell layer are separately obtained; then the precursor material mixed solution is dropped into the core particle dispersion, and a resulting mixture were heated to promote the deposition of the precursor material onto the surfaces of the core particles so as to form a single shell layer, whereby obtaining the electrophoretic particles.
  • the organic solvent includes but is not limited to methanol and ethanol.
  • Core particles and a shell layer material precursor were provided according to the electrophoretic particle according to Example 2.
  • the electrophoretic particle comprises a shell layer and a core layer wrapped in the shell layer.
  • the core layer comprises a plurality of core particles, and voids exist among the plurality of core particles.
  • the plurality of core particles are magnesium oxide, and the shell layer is titanium dioxide.
  • Each of the plurality of core particles has a particle size of 35 nm; the electrophoretic particle has a particle size of 500 nm; a volume of the core layer accounts for 50% of the volume of the electrophoretic particle, and a volume of the voids account for 12% of the volume of the core layer.
  • the preparation method included the same operations as in Example 1 except that ammonia water having a concentration of 50% was replaced with hexamethylenetetramine to obtain the corresponding nanoparticles in core-shell structures.
  • the electrophoretic particle comprises a shell layer and a core layer wrapped in the shell layer.
  • the core layer comprises a plurality of core particles, and voids exist among the plurality of core particles.
  • the plurality of core particles are silicon dioxide, and the shell layer is titanium dioxide.
  • Each of the plurality of core particles has a particle size of 45 nm; the electrophoretic particle has a particle size of 800 nm; a volume of the core layer accounts for 70% of the volume of the electrophoretic particle, and a volume of the voids account for 5% of the volume of the core layer.
  • the preparation method included the same operations as in Example 2, except that ammonia water having a concentration of 50% was replaced by hexamethylenetetramine, and the dropping rate of the ethanol solution was changed from 0.1 mL/s to 0.12 mL/s to obtain the corresponding nanoparticles in core-shell structures.
  • the electrophoretic particle comprises a shell layer and a core layer wrapped in the shell layer.
  • the core layer comprises a plurality of core particles, and voids exist among the plurality of core particles.
  • the plurality of core particles are silicon dioxide, and the shell layer is titanium dioxide.
  • Each of the plurality of core particles has a particle size of 50 nm; the electrophoretic particle has a particle size of 1000 nm; a volume of the core layer accounts for 80% of the volume of the electrophoretic particle, and a volume of the voids account for 15% of the volume of the core layer.
  • the electrophoretic particles are nanoparticles having single-core type core-shell structures, the core particle is silicon dioxide, and the shell layer is titanium dioxide; the core particle has a particle size of 100 nm; and the shell layer has a thickness of 200 nm.
  • the preparation method included the same operations as in Example 2 to obtain the corresponding nanoparticles in the single-core type core-shell structures.

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EP22906662.6A 2021-12-17 2022-12-15 Particule électrophorétique et procédé de préparation associé et son application Pending EP4394002A4 (fr)

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TWI229115B (en) * 2002-02-11 2005-03-11 Sipix Imaging Inc Core-shell particles for electrophoretic display
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